医生将淀粉样变性分为三种主要类型。
目的探讨咽喉部淀粉样变性的临床特点。
Objective To study the clinical manifestations of pharyngeal and laryngeal amyloidosis.
局限性淀粉样变性18例。
最右边呈现粉红色透明样，为淀粉样变性。
At the far right is pink hyaline material with the appearance of amyloid.
目的分析探讨淀粉样变性心肌病的临床特点。
Objective: To investigate the clinical characteristics of cardiac amyloidosis.
目的探讨肾脏淀粉样变性的临床病理学特点。
Objective To investigate the clinicopathologic characteristics of renal amyloidosis.
【译】成像：心脏淀粉样变性患者CMR成像。
原发性肾淀粉样变性11例，继发性肾淀粉样变性4例。
Primary kidney amyloidosis was found in 11 cases, and secondary kidney amyloidosis in 4 cases.
肾脏淀粉样变性是一种能增加肾脏体积的慢性肾脏疾病。
Here is a chronic renal disease that may actually increase the size of the kidney. This is amyloidosis.
目的探讨淀粉样变性肾病的病理学特征、诊断及鉴别诊断。
Purpose To investigate the pathological characteristics, diagnosis and differential diagnosis of amyloid nephropathy.
淀粉样变性，异常蛋白在组织中积聚的一种疾病，可发生在CD。
Amyloidosis, a disease where abnormal proteins are deposited in tissues, can occur in CD.
同时也多多注意脑组织中的小血管，看是否存在小血管壁的淀粉样变性。
Also do pay attention to small blood vessels in cortex and see if there is any features of cerebral amyloid angiopathy.
为寻求其他专家的不同意见，波夫莱特在网上查询淀粉样变性方面的专家。
In search of a second opinion, Poblete tracked down amyloidosis experts on the Internet.
结论：心脏淀粉样变性患者早期即出现舒张功能障碍，而收缩功能尚可维持正常。
Conclusion: the diastolic dysfunction appears in the early stage in cardiac amyloidosis while the systolic function keeps normal.
还有一部分(比例不确定)病人可能占10%，有第三种异常蛋白——淀粉样变性。
An uncertain proportion of patients, possibly about 10 per cent, have a third protein abnormality - amyloidosis.
还有一部分(比例不确定)病人可能占10%，有第三种异常蛋白——淀粉样变性。
An uncertain proportion of patients, possibly about 10 per cent, have a third protein abnormality-amyloidosis.
骨髓外浸润、眶内及皮肤浸润多见，肾功能损害、高钙血症、淀粉样变性的发生率较高。
Extramedullary infiltration, orbit and skin infiltration were more common, and the incidence of renal function impairment, hypercalcemia, and amyloidosis was higher.
目的：探讨原发性系统性淀粉样变性并发凝血因子x缺乏的临床特征、发病机制及治疗方法。
Objective: to investigate the clinical feature, pathogenesis, and therapy of Primary systemic amyloidosis with acquired factor-X deficiency.
克罗斯患有一种其家族特有的淀粉样变性疾病，它使肝脏无法分解一种叫做转体基因的蛋白。
Cross's disease, familial amyloidosis, prevents the liver from breaking down a protein called transthyretin.
当淀粉样蛋白由免疫球蛋白轻链组成时，那么它就是“免疫细胞衍生性淀粉样变性”，当它来自于血清淀粉相关蛋白时，就是“反应性系统性淀粉样变性”。
When the amyloid protein is made up of immunoglobulin light chains, then it is "AL amyloid" and when it is derived from serum amyloid-associated protein, then it is "AA amyloid.
当淀粉样蛋白由免疫球蛋白轻链组成时，那么它就是“免疫细胞衍生性淀粉样变性”，当它来自于血清淀粉相关蛋白时，就是“反应性系统性淀粉样变性”。
When the amyloid protein is made up of immunoglobulin light chains, then it is "AL amyloid" and when it is derived from serum amyloid-associated protein, then it is "AA amyloid.
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